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nsv6556944

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,065,306

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 24905 SVs from 129 studies. See in: genome view    
    Submitted genomic130,985,407-137,050,712Question Mark
    Overlapping variant regions from other studies: 24706 SVs from 129 studies. See in: genome view    
    Remapped(Score: Good):133,860,794-139,945,164Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6556944Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9130,985,407137,050,712
    nsv6556944RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9133,860,794139,945,164

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18280062inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18280062Submitted genomicNC_000009.12:g.130
    985407_137050712in
    v
    GRCh38 (hg38)NC_000009.12Chr9130,985,407137,050,712
    nssv18280062RemappedGoodNC_000009.11:g.133
    860794_139945164in
    v
    GRCh37.p13First PassNC_000009.11Chr9133,860,794139,945,164

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18280062<0.001239304
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